Variant report

Variant	nsv908566
Chromosome Location	chr17:45465735-45569714
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:428)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45505316-45506040	HepG2	liver:	n/a	n/a
2	ATF2	chr17:45569649-45570147	GM12878	blood:	n/a	n/a
3	ATF3	chr17:45569636-45570283	A549	lung:	n/a	n/a
4	BATF	chr17:45569645-45570111	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:45504891-45505246	GM12878	blood:	n/a	n/a
6	BCLAF1	chr17:45569636-45570116	GM12878	blood:	n/a	chr17:45569672-45569681
7	CBX3	chr17:45569445-45570802	K562	blood:	n/a	n/a
8	CBX3	chr17:45569612-45570280	K562	blood:	n/a	n/a
9	CEBPB	chr17:45482271-45482609	K562	blood:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
10	CEBPB	chr17:45482316-45482557	A549	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
11	CEBPB	chr17:45505310-45505563	HepG2	liver:	n/a	n/a
12	CEBPB	chr17:45549562-45549781	HepG2	liver:	n/a	n/a
13	CEBPB	chr17:45493468-45493688	K562	blood:	n/a	chr17:45493564-45493575
14	CEBPB	chr17:45493445-45493683	A549	lung:	n/a	chr17:45493564-45493575
15	CEBPB	chr17:45482340-45482579	IMR90	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
16	CEBPB	chr17:45482269-45482596	HepG2	liver:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
17	CEBPB	chr17:45491776-45491931	K562	blood:	n/a	n/a
18	CEBPB	chr17:45569419-45570032	GM12878	blood:	n/a	n/a
19	CEBPB	chr17:45493466-45493668	HepG2	liver:	n/a	chr17:45493564-45493575
20	CEBPD	chr17:45569615-45569858	HepG2	liver:	n/a	n/a
21	CEBPD	chr17:45569533-45570107	K562	blood:	n/a	n/a
22	CEBPD	chr17:45569673-45569842	HepG2	liver:	n/a	n/a
23	CREB1	chr17:45569704-45570296	A549	lung:	n/a	n/a
24	CTCF	chr17:45480800-45480950	AG09319	gingival:	n/a	n/a
25	CTCF	chr17:45500980-45501130	GM12865	blood:	n/a	n/a
26	CTCF	chr17:45501060-45501210	GM12871	blood:	n/a	n/a
27	CTCF	chr17:45541176-45541214	LNCaP	prostate:	n/a	n/a
28	CTCF	chr17:45480700-45480850	HCT-116	colon:	n/a	n/a
29	CTCF	chr17:45482723-45482749	GM10248	blood:	n/a	n/a
30	CTCF	chr17:45501140-45501290	HEK293	kidney:	n/a	n/a
31	CTCF	chr17:45501637-45501674	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr17:45527137-45527166	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr17:45513628-45513693	Lung_OC	lung:	n/a	n/a
34	CTCF	chr17:45545460-45545610	BJ	skin:	n/a	n/a
35	CTCF	chr17:45501628-45501635	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr17:45545360-45545510	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr17:45501124-45501145	GM12891	blood:	n/a	n/a
38	CTCF	chr17:45480800-45480950	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr17:45507446-45507452	A549	lung:	n/a	n/a
40	CTCF	chr17:45500839-45500928	MCF-7	breast:	n/a	n/a
41	CTCF	chr17:45545592-45545679	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr17:45501060-45501210	GM12872	blood:	n/a	n/a
43	CTCF	chr17:45501099-45501153	A549	lung:	n/a	n/a
44	CTCF	chr17:45500854-45500948	MCF-7	breast:	n/a	n/a
45	CTCF	chr17:45501040-45501190	GM12874	blood:	n/a	n/a
46	CTCF	chr17:45545440-45545590	HepG2	liver:	n/a	n/a
47	CTCF	chr17:45555719-45555780	GM20000	blood:	n/a	n/a
48	CTCF	chr17:45501146-45501167	GM12891	blood:	n/a	n/a
49	CTCF	chr17:45529856-45529896	GM13976	blood:	n/a	n/a
50	CTCF	chr17:45491577-45491639	Fibrobl	skin:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45501697-45501747	BE2_C	brain:	n/a
2	chr17:45501697-45501747	BE2_C	brain:	n/a
3	chr17:45501030-45501080	PANC-1	pancreas:	n/a
4	chr17:45566670-45566720	NHBE	bronchial:	n/a
5	chr17:45501697-45501747	PANC-1	pancreas:	n/a
6	chr17:45502151-45502201	AoSMC	blood vessel:	n/a
7	chr17:45566670-45566720	K562	blood:	n/a
8	chr17:45501242-45501292	SKMC	muscle:	n/a
9	chr17:45501697-45501747	SKMC	muscle:	n/a
10	chr17:45501628-45501678	Hela-S3	cervix:	n/a
11	chr17:45566670-45566720	IMR90	lung:	fetal
12	chr17:45505249-45505299	AG09319	gingival:	n/a
13	chr17:45501030-45501080	NB4	blood:	n/a
14	chr17:45501242-45501292	SK-N-SH_RA	brain:	n/a
15	chr17:45501628-45501678	T-47D	breast:	n/a
16	chr17:45501030-45501080	NT2-D1	testis:	n/a
17	chr17:45501628-45501678	Hepatocyte	liver:	n/a
18	chr17:45501697-45501747	HEK293	kidney:	embryo
19	chr17:45505249-45505299	SKMC	muscle:	n/a
20	chr17:45501697-45501747	PrEC	prostate:	n/a
21	chr17:45505249-45505299	AG04449	skin:	fetal
22	chr17:45566670-45566720	AoSMC	blood vessel:	n/a
23	chr17:45501030-45501080	PFSK-1	brain:	n/a
24	chr17:45501628-45501678	LNCaP	prostate:	n/a
25	chr17:45566670-45566720	AG09309	skin:	n/a
26	chr17:45501697-45501747	AG04449	skin:	fetal
27	chr17:45501628-45501678	NT2-D1	testis:	n/a
28	chr17:45566670-45566720	SKMC	muscle:	n/a
29	chr17:45502151-45502201	HRE	kidney:	n/a
30	chr17:45502151-45502201	A549	lung:	n/a
31	chr17:45501242-45501292	SAEC	small airway:	n/a
32	chr17:45566670-45566720	GM19239	blood:	n/a
33	chr17:45501628-45501678	AG10803	skin:	n/a
34	chr17:45566670-45566720	H1-hESC	embryonic stem cell:	embryo
35	chr17:45501242-45501292	HMEC	breast:	n/a
36	chr17:45501697-45501747	ovcar-3	ovarian:	n/a
37	chr17:45501697-45501747	SK-N-SH_RA	brain:	n/a
38	chr17:45501628-45501678	HL-60	blood:	n/a
39	chr17:45501242-45501292	A549	lung:	n/a
40	chr17:45502151-45502201	ECC-1	luminal epithelium:	n/a
41	chr17:45501030-45501080	GM19239	blood:	n/a
42	chr17:45505249-45505299	ECC-1	luminal epithelium:	n/a
43	chr17:45501628-45501678	HepG2	liver:	n/a
44	chr17:45501242-45501292	MCF10A-Er-Src	breast:	n/a
45	chr17:45566670-45566720	NHDF-neo	bronchial:	n/a
46	chr17:45505249-45505299	HMEC	breast:	n/a
47	chr17:45505249-45505299	HRE	kidney:	n/a
48	chr17:45566670-45566720	SAEC	small airway:	n/a
49	chr17:45501697-45501747	HEEpiC	esophagus:	n/a
50	chr17:45501628-45501678	Jurkat	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45567844..45569771-chr17:45694216..45696585,2	K562	blood:
2	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
3	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:
4	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
5	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
6	chr17:45568465..45570063-chr17:45725230..45727294,2	K562	blood:
7	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
8	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:
9	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
10	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
11	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
12	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
13	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
14	chr17:45499733..45501782-chr17:45502052..45504438,2	K562	blood:
15	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
16	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
17	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:
18	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
19	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C17orf57-1	chr17:45522601-45522883	NONHSAT054305
2	lnc-AC040934.1-1	chr17:45500728-45500892	ENSG00000253347.1
3	lnc-AC040934.1-1	chr17:45486688-45487035	ENSG00000253347.1

No data

Variant related genes	Relation type
ENSG00000253347	TF binding region
MRPL45P2	TF binding region
ENSG00000253347	CpG island
MRPL45P2	CpG island
ENSG00000253347	chromatin interactions
ENSG00000263766	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000141279	chromatin interactions

Extended variants
information (count: 3507 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3507 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11868497	chr17:45465735-45465736	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572254989	chr17:45465761-45465762	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs181149382	chr17:45465805-45465806	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368787705	chr17:45465833-45465834	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529545737	chr17:45465834-45465835	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150379573	chr17:45465890-45465891	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73985161	chr17:45465909-45465910	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11870948	chr17:45465943-45465944	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs186497522	chr17:45465978-45465979	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79293589	chr17:45466085-45466086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570401188	chr17:45466198-45466199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12946599	chr17:45466230-45466231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535995509	chr17:45466248-45466249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199883288	chr17:45466282-45466283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562302592	chr17:45466285-45466286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191014611	chr17:45466328-45466329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181029255	chr17:45466334-45466335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552886128	chr17:45466396-45466397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185343990	chr17:45466406-45466407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566410659	chr17:45466459-45466460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144522822	chr17:45466466-45466467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373064412	chr17:45466477-45466478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577392264	chr17:45466486-45466487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138010527	chr17:45466524-45466525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78037476	chr17:45466557-45466558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76787451	chr17:45466558-45466559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80028537	chr17:45466559-45466560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555106374	chr17:45466614-45466615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35865814	chr17:45466672-45466673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190843268	chr17:45466704-45466705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73324443	chr17:45466771-45466772	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs114693451	chr17:45466828-45466829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78415837	chr17:45466874-45466875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540605346	chr17:45466921-45466922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551358125	chr17:45466945-45466946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560788907	chr17:45466962-45466963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529578780	chr17:45466964-45466965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543253422	chr17:45467022-45467023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563026063	chr17:45467055-45467056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531931255	chr17:45467133-45467134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537086785	chr17:45467169-45467170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550446884	chr17:45467188-45467189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370009972	chr17:45467261-45467262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113069711	chr17:45467307-45467308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201309521	chr17:45467308-45467309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199657645	chr17:45467309-45467310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200397614	chr17:45467310-45467311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73985162	chr17:45467311-45467312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535881562	chr17:45467345-45467346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149091996	chr17:45467355-45467356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:1150 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45402200-45500800	Weak transcription	Aorta	Aorta
2	chr17:45411600-45468200	Weak transcription	Left Ventricle	heart
3	chr17:45450800-45470400	Weak transcription	Liver	Liver
4	chr17:45460600-45467400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr17:45460800-45466600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr17:45461400-45466800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr17:45461400-45500400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr17:45461600-45475200	Weak transcription	Colon Smooth Muscle	Colon
9	chr17:45461600-45500600	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr17:45461600-45500600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr17:45462600-45468000	Weak transcription	Fetal Muscle Leg	muscle
12	chr17:45463000-45466000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr17:45463200-45465800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr17:45463200-45465800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr17:45463200-45466800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr17:45463400-45466400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr17:45463400-45467800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr17:45463600-45470000	Weak transcription	Spleen	Spleen
19	chr17:45463600-45473400	Weak transcription	Fetal Brain Male	brain
20	chr17:45463800-45468200	Weak transcription	HepG2	liver
21	chr17:45463800-45468800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr17:45463800-45477800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr17:45464000-45470600	Weak transcription	Gastric	stomach
24	chr17:45464000-45481400	Weak transcription	Lung	lung
25	chr17:45464000-45487800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr17:45464200-45466000	Weak transcription	Primary B cells from peripheral blood	blood
27	chr17:45464200-45466600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr17:45464200-45496800	Weak transcription	Fetal Intestine Small	intestine
29	chr17:45464400-45477000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr17:45464400-45493800	Weak transcription	Ovary	ovary
31	chr17:45464600-45470000	Weak transcription	Fetal Stomach	stomach
32	chr17:45465000-45465800	Strong transcription	Primary T cells from cord blood	blood
33	chr17:45465200-45465800	Strong transcription	Fetal Muscle Trunk	muscle
34	chr17:45465400-45466200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr17:45465600-45496800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr17:45465600-45500200	Weak transcription	Primary B cells from cord blood	blood
37	chr17:45465800-45468200	Weak transcription	Primary T cells from cord blood	blood
38	chr17:45465800-45470000	Weak transcription	Fetal Muscle Trunk	muscle
39	chr17:45465800-45471800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr17:45466000-45466400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr17:45466000-45467000	Strong transcription	Primary B cells from peripheral blood	blood
42	chr17:45466000-45468400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr17:45466400-45466800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr17:45466400-45466800	Weak transcription	Right Ventricle	heart
45	chr17:45466800-45469400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr17:45466800-45499600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr17:45467000-45473200	Weak transcription	Primary B cells from peripheral blood	blood
48	chr17:45470400-45500400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr17:45471800-45472600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr17:45472000-45474800	Weak transcription	NHDF-Ad	bronchial

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